1432601-99-4

Basic information

• Product Name: (R)-tert-butyl 2-((R)-4-methyl-3-oxocyclohex-1-enyl)pent-4-enoate
• Synonyms: (R)-tert-butyl 2-((R)-4-methyl-3-oxocyclohex-1-enyl)pent-4-enoate
• CAS NO: 1432601-99-4
• Molecular Weight: 264.365
• Mol File: 1432601-99-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-tert-butyl 2-((R)-4-methyl-3-oxocyclohex-1-enyl)pent-4-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-tert-butyl 2-((R)-4-methyl-3-oxocyclohex-1-enyl)pent-4-enoate(1432601-99-4)
• EPA Substance Registry System: (R)-tert-butyl 2-((R)-4-methyl-3-oxocyclohex-1-enyl)pent-4-enoate(1432601-99-4)

Safety Data

• Hazardous Substances Data: 1432601-99-4(Hazardous Substances Data)

Upstream product

• 1694-31-1 tert-butyl acetoacetate 
• 39149-69-4 tert-butyl 2-acetyl-4-pentenoate 
• 6610-21-5 6-methylcyclohex-2-en-1-one 
• 1426247-71-3 tert-butyl 2-diazopent-4-enoate 
• 62392-84-1 (+)-(R)-6-methylcyclohex-2-en-1-one 

Relevant articles and documents

Method of stereoselectively synthesizing β-functionalized cyclic Enone

The present invention provides a method for stereoselectively synthesizing β-functionalized cyclic enone. The β-functionalized cyclic enone is stereoseletively synthesized by making non-functionalized cyclic enone react with diazoacetate in the presence of an oxazabororidium ion catalyst. According to the method, β-functionalized cyclic enone can be stereoselectively synthesized with high efficiency by a single step.